NDC 43596-0206 Concentre Total Base Serum Base De Maquillaje Ultra-fluid Foundation Spf 25 Capuccino 310-c
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Product Details
What is NDC 43596-0206?
What are the uses for Concentre Total Base Serum Base De Maquillaje Ultra-fluid Foundation Spf 25 Capuccino 310-c?
Which are Concentre Total Base Serum Base De Maquillaje Ultra-fluid Foundation Spf 25 Capuccino 310-c UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Concentre Total Base Serum Base De Maquillaje Ultra-fluid Foundation Spf 25 Capuccino 310-c Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- NYLON-12 (UNII: 446U8J075B)
- ALCOHOL (UNII: 3K9958V90M)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)
- LECITHIN, SUNFLOWER (UNII: 834K0WOS5G)
- HEXYL LAURATE (UNII: 4CG9F9W01Q)
- TROMETHAMINE (UNII: 023C2WHX2V)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SILANEDIOL SALICYLATE (UNII: C054DF30K0)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- MAITAKE (UNII: A1U5YJI0Z8)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CERAMIDE NP (UNII: 4370DF050B)
- ISODODECANE (UNII: A8289P68Y2)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- METHYLPROPANEDIOL (UNII: N8F53B3R4R)
- GLYCERIN (UNII: PDC6A3C0OX)
- HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)
- PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
- WATER (UNII: 059QF0KO0R)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[6] What is the FDA Application Number? - This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".